What pattern of curved arrow pushing is the second step of this reaction? O₂N. O₂N H O proton transfer O loss of leaving group O nucleophilic attack O rearrangement
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- Which products are most likely to form in this reaction? NH2 H2N NaNH2 NH2 liq. NH3 II O1, II & II O II & II O1& || OI & II4. Draw the product of the following Reactions. Excess HI Heat ? 1. Br₂, H₂O 2. NaOH 1. NaOH 2. H₂O ? ?Complete the reaction map by matching A-E with the given choices. H2 H2 B E Pt Cla Na in lig NH3 он + но Match each item to a choice A
- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. H N. Br2 Br • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. IZPLEASE HELPBy taking into account electronegativity differences, draw the products formed by heterolysis of the carbon–heteroatom bond in each molecule. Classify the organic reactive intermediate as a carbocation or a carbanion.
- PS6-5. Label each step of the mechanism as either a proton transfer (PT), nucleophilic attack (NA), loss of leaving group (LOLG), or carbocation rearrangement (CR). *O* :ÖH b. :ÖR HO. *O* LOH H₂O HO PS6-6. Label each step of the mechanism as either a proton transfer (PT), nucleophilic attack (NA), loss of leaving group (LOLG), or carbocation rearrangement (CR). Draw curved arrows for each step. H R OH -H₂O 'H H :ÖH مته مرة ÖR :ÖH s-settet H :ÖH :ÖH *O* 14-0-H Fön :ÖHConsider the following SN2 reaction, C NaOCH₂ CH₂OH OCH what would happen if the concentration of NaOCH 3 was doubled? Elimination would become the major reaction. The rate of reaction would be halved. The rate of reaction would stay the same. The rate of reaction would double.Complete the following reaction